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Refinado por: Nome da Publicação: American Journal of Medical Genetics remover
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1
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
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Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology

Klaus Zerres Gabi Mücher; Jutta Becker; Carsten Steinkmamm; Sabine Rudnik Schöneborn; Päivi Heikkilä; Juhani Rapola; Riitta Salonen; Gregory G Germino; Luiz Fernando Onuchic; Stefan Somlo; Ellis D Avner; Leight A Harman; John M Stockwin; Lisa M. Guay Woodford

American Journal of Medical Genetics v. 76, n. 02, p. 137-144, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

2
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prenatal diagnosis of autosomal recessive polycystic Kidney disease (ARPKD) molecular genetcs, clinical experience, and fetal morphology

Klaus Zerres Gabi Mücher; Jutta Becker; Carsten Steinkmamm; Sabine Rudnik Schöneborn; Päivi Heikkilä; Juhani Rapola; Riitta Salonen; Gregory G Germino; Luiz Fernando Onuchic; Stefan Somlo; Ellis D Avner; Leight A Harman; John M Stockwin; Lisa M. Guay Woodford

American Journal of Medical Genetics v. 76, n. 02, p. 137-144, 1998

1998

Item não circula. Consulte sua biblioteca.(Acessar)

3
Increased chromosomal breakage in tourette syndrome predicts the possibility of variable multiple gene involvement in spectrum phenotypes: Preliminary findings and hypothesis
Increased chromosomal breakage in tourette syndrome predicts the possibility of variable multiple gene involvement in spectrum phenotypes: Preliminary findings and hypothesis
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Increased chromosomal breakage in tourette syndrome predicts the possibility of variable multiple gene involvement in spectrum phenotypes: Preliminary findings and hypothesis

Gericke, George S. ; Simonic, Ingrid ; Cloete, Elma ; Buckle, Cecile ; Becker, Piet J.

American journal of medical genetics, 1995-10, Vol.60 (5), p.444-447 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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4
Increased expression of aphidicolin-induced common fragile sites in Tourette syndrome: The key to understand the genetics of comorbid phenotypes?
Increased expression of aphidicolin-induced common fragile sites in Tourette syndrome: The key to understand the genetics of comorbid phenotypes?
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Increased expression of aphidicolin-induced common fragile sites in Tourette syndrome: The key to understand the genetics of comorbid phenotypes?

Gericke, George S. ; Simonic, Ingrid ; Cloete, Elma ; Becker, Piet J.

American journal of medical genetics, 1996-02, Vol.67 (1), p.25-30 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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5
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology
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Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology

Zerres, Klaus ; Mücher, Gabi ; Becker, Jutta ; Steinkamm, Carsten ; Rudnik-Schöneborn, Sabine ; Heikkilä, Päivi ; Rapola, Juhani ; Salonen, Riitta ; Germino, Gregory G. ; Onuchic, Luiz ; Somlo, Stefan ; Avner, Ellis D. ; Harman, Leigh A. ; Stockwin, John M. ; Guay-Woodford, Lisa M.

American journal of medical genetics, 1998-03, Vol.76 (2), p.137-144 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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6
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome
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Oligohydramnios hampering prenatal diagnosis of Meckel syndrome

Verjaal, Marianne ; Meyer, Adriaan H. ; Becker-Bloemkolk, Mies J. ; Leschot, Nico J. ; der Weduwen, Johanna J. ; Gras, Joop G. F. M.

American journal of medical genetics, 1980, Vol.7 (1), p.85-86 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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7
Familial ovarian germ cell cancer: Report and review
Familial ovarian germ cell cancer: Report and review
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Familial ovarian germ cell cancer: Report and review

Stettner, Amy R. ; Hartenbach, Ellen M. ; Schink, Julian C. ; Huddart, Robert ; Becker, Joanne ; Pauli, Richard ; Long, Robert ; Laxova, Renata

American journal of medical genetics, 1999-05, Vol.84 (1), p.43-46

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
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Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma

Niemann, Stephan ; Becker-Follmann, Johannes ; Nürnberg, Gudrun ; Rüschendorf, Franz ; Sieweke, Nicole ; Hügens-Penzel, Monika ; Traupe, Horst ; Wienker, Thomas F. ; Reis, André ; Müller, Ulrich

American journal of medical genetics, 2001-01, Vol.98 (1), p.32-36 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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Deste Autor:

  1. Somlo, S
  2. Mücher, G
  3. Stockwin, J
  4. Germino, G
  5. Zerres, K

Neste Assunto:

  1. Female
  2. Humans
  3. Genetics & Heredity
  4. Life Sciences & Biomedicine
  5. Male

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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